A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3077



Internal ID15547650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:156540942..156560239hg38UCSC Ensembl
Outerchr1:156510734..156530031hg19UCSC Ensembl
Outerchr1:154777358..154796655hg18UCSC Ensembl
Outerchr1:153323807..153343104hg17UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3819298
hg1919298
hg1819298
hg1719298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4730, nssv7086
SamplesNA12156, NA19129
Known GenesIQGAP3
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv3077
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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